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American Journal of Hematology|June 1, 1997
Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemiaC Camaschella, A C Kattamis, D Petroni, et al.
Proceedings of the Association of American Physicians|May 1, 1996
Gaucher disease: four families with previously undescribed mutationsE Beutler, T Gelbart, D Balicki, et al.
British Medical Journal|July 26, 1980
Haemoglobin Bart's hydrops syndrome in GreeceC Kattamis, A Metaxotou-Mavromati, E Tsiarta, et al.
Transfusion|July 1, 1997
The presurgical management with erythrocytapheresis of a patient with a high-oxygen-affinity, unstable Hb variant (Hb Bryn Mawr)P J Larson, D F Friedman, M P Reilly, et al.
Blood|February 1, 1986
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in GreeksP G Waber, M A Bender, R E Gelinas, et al.
Magnetic Resonance Imaging|January 1, 1995
Assessment of liver iron overload by T2-quantitative magnetic resonance imaging: correlation of T2-QMRI measurements with serum ferritin concentration and histologic grading of siderosisO G Papakonstantinou, T G Maris, V Kostaridou, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Genetic and molecular diversity in nondeletion Hb H diseaseD R Higgs, L Pressley, B Aldridge, et al.
British Journal of Haematology|December 1, 1979
A comparison of the homozygous states for G gamma and G gamma A gamma delta beta thalassaemiaA B Amin, N L Pandya, P P Diwin, et al.
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